Canonical Allele Identifier: CA8700149
Gene: ACE HGNC NCBI

Linked Data

dbSNP Id: rs377172559

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63489048C>T , CM000679.2:g.63489048C>T GRCh38
NC_000017.10:g.61566409C>T , CM000679.1:g.61566409C>T GRCh37
NC_000017.9:g.58920141C>T NCBI36
NG_011648.1:g.16976C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.2557C>T MANE Select ENSP00000290866.4:p.His853Tyr
ENST00000290863.10:c.835C>T ENSP00000290863.6:p.His279Tyr
ENST00000290866.9:c.2557C>T ENSP00000290866.4:p.His853Tyr
ENST00000413513.7:c.835C>T ENSP00000392247.3:p.His279Tyr
ENST00000428043.5:c.2557C>T ENSP00000397593.2:p.His853Tyr
ENST00000577647.2:c.835C>T ENSP00000464149.1:p.His279Tyr
ENST00000578839.5:c.*519+257C>T ENSP00000462110.2:n.*519+257C>T
ENST00000579314.5:c.*286C>T ENSP00000462599.1:n.*286C>T
ENST00000582005.5:c.*477C>T ENSP00000462002.1:n.*477C>T
ENST00000582761.1:c.325C>T ENSP00000462909.1:p.His109Tyr
ENST00000584865.5:n.503C>T
NM_000789.3:c.2557C>T NP_000780.1:p.His853Tyr
NM_001178057.1:c.835C>T NP_001171528.1:p.His279Tyr
NM_152830.2:c.835C>T NP_690043.1:p.His279Tyr
XM_005257110.1:c.2008C>T XP_005257167.1:p.His670Tyr
XM_006721737.2:c.895C>T XP_006721800.2:p.His299Tyr
XM_006721737.3:c.895C>T XP_006721800.2:p.His299Tyr
NM_000789.4:c.2557C>T MANE Select NP_000780.1:p.His853Tyr
NM_001178057.2:c.835C>T NP_001171528.1:p.His279Tyr
NM_152830.3:c.835C>T NP_690043.1:p.His279Tyr
NM_001382700.1:c.1990C>T NP_001369629.1:p.His664Tyr
NM_001382701.1:c.1705C>T NP_001369630.1:p.His569Tyr
NM_001382702.1:c.379+257C>T NP_001369631.1:n.379+257C>T
NR_168483.1:n.935C>T